Canonical Allele Identifier: PA2829983728
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406068
ClinVar RCV Id: RCV000572414 RCV000589806 RCV001086420
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Ile1711Met
CA054841
NM_021055.3:c.5133C>G